These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
320 related articles for article (PubMed ID: 21150918)
1. Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China. Sun Y; Chen J; Sun H; Cheng J; Li J; Lu Y; Lu Y; Jin Z; Zhu Y; Ouyang X; Yan D; Dai P; Han D; Yang W; Wang R; Liu X; Yuan H J Hum Genet; 2011 Jan; 56(1):64-70. PubMed ID: 21150918 [TBL] [Abstract][Full Text] [Related]
2. Identification of a MYO7A mutation in a large Chinese DFNA11 family and genotype-phenotype review for DFNA11. Li L; Yuan H; Wang H; Guan J; Lan L; Wang D; Zong L; Liu Q; Han B; Huang D; Wang Q Acta Otolaryngol; 2018 May; 138(5):463-470. PubMed ID: 29400105 [TBL] [Abstract][Full Text] [Related]
3. Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11). Bolz H; Bolz SS; Schade G; Kothe C; Mohrmann G; Hess M; Gal A Hum Mutat; 2004 Sep; 24(3):274-5. PubMed ID: 15300860 [TBL] [Abstract][Full Text] [Related]
4. Phenotype of DFNA11: a nonsyndromic hearing loss caused by a myosin VIIA mutation. Tamagawa Y; Ishikawa K; Ishikawa K; Ishida T; Kitamura K; Makino S; Tsuru T; Ichimura K Laryngoscope; 2002 Feb; 112(2):292-7. PubMed ID: 11889386 [TBL] [Abstract][Full Text] [Related]
5. Identification and functional study of a new missense mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11). Sang Q; Yan X; Wang H; Feng R; Fei X; Ma D; Xing Q; Li Q; Zhao X; Jin L; He L; Li H; Wang L PLoS One; 2013; 8(1):e55178. PubMed ID: 23383098 [TBL] [Abstract][Full Text] [Related]
6. [Genetic and audiological characters of a Chinese family with non-syndromic hereditary hearing loss]. Jin Z; Cheng J; Lu Y; Li J; Sun Y; Yuan H; Han D Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2011 Feb; 25(4):158-61. PubMed ID: 21563462 [TBL] [Abstract][Full Text] [Related]
7. Genetic analysis of a four generation Indian family with Usher syndrome: a novel insertion mutation in MYO7A. Kumar A; Babu M; Kimberling WJ; Venkatesh CP Mol Vis; 2004 Nov; 10():910-6. PubMed ID: 15592175 [TBL] [Abstract][Full Text] [Related]
8. Novel compound heterozygous mutations in MYO7A gene associated with autosomal recessive sensorineural hearing loss in a Chinese family. Ma Y; Xiao Y; Zhang F; Han Y; Li J; Xu L; Bai X; Wang H Int J Pediatr Otorhinolaryngol; 2016 Apr; 83():179-85. PubMed ID: 26968074 [TBL] [Abstract][Full Text] [Related]
9. Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11). Luijendijk MW; Van Wijk E; Bischoff AM; Krieger E; Huygen PL; Pennings RJ; Brunner HG; Cremers CW; Cremers FP; Kremer H Hum Genet; 2004 Jul; 115(2):149-56. PubMed ID: 15221449 [TBL] [Abstract][Full Text] [Related]
10. Mutations in the myosin VIIA gene cause non-syndromic recessive deafness. Liu XZ; Walsh J; Mburu P; Kendrick-Jones J; Cope MJ; Steel KP; Brown SD Nat Genet; 1997 Jun; 16(2):188-90. PubMed ID: 9171832 [TBL] [Abstract][Full Text] [Related]
11. Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis gene. Yan X; Wang X; Wang Z; Sun S; Chen G; He Y; Mo JQ; Li R; Jiang P; Lin Q; Sun M; Li W; Bai Y; Zhang J; Zhu Y; Lu J; Yan Q; Li H; Guan MX J Med Genet; 2011 Oct; 48(10):682-90. PubMed ID: 21931169 [TBL] [Abstract][Full Text] [Related]
12. Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation. Hildebrand MS; Thorne NP; Bromhead CJ; Kahrizi K; Webster JA; Fattahi Z; Bataejad M; Kimberling WJ; Stephan D; Najmabadi H; Bahlo M; Smith RJ Clin Genet; 2010 Jun; 77(6):563-71. PubMed ID: 20132242 [TBL] [Abstract][Full Text] [Related]
13. Genotype-phenotype correlation for DFNA22: characterization of non-syndromic, autosomal dominant, progressive sensorineural hearing loss due to MYO6 mutations. Topsakal V; Hilgert N; van Dinther J; Tranebjaerg L; Rendtorff ND; Zarowski A; Offeciers E; Van Camp G; van de Heyning P Audiol Neurootol; 2010; 15(4):211-20. PubMed ID: 19893302 [TBL] [Abstract][Full Text] [Related]
14. Clinical Profiles of DFNA11 at Diverse Stages of Development and Aging in a Large Family Identified by Linkage Analysis. Yamamoto N; Mutai H; Namba K; Goto F; Ogawa K; Matsunaga T Otol Neurotol; 2020 Jul; 41(6):e663-e673. PubMed ID: 32097363 [TBL] [Abstract][Full Text] [Related]
15. [Gene mapping for autosomal dominant nonsyndromic hearing loss DFNA11]. Yuan H; Han DY; Wang QJ; Zong L; Zhao YL Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2007 Jun; 42(6):422-7. PubMed ID: 17702415 [TBL] [Abstract][Full Text] [Related]
16. In search of the DFNA11 myosin VIIA low- and mid-frequency auditory genetic modifier. Kallman JC; Phillips JO; Bramhall NF; Kelly JP; Street VA Otol Neurotol; 2008 Sep; 29(6):860-7. PubMed ID: 18667942 [TBL] [Abstract][Full Text] [Related]
17. Identification of a novel mutation in the myosin VIIA motor domain in a family with autosomal dominant hearing loss (DFNA11). Di Leva F; D'Adamo P; Cubellis MV; D'Eustacchio A; Errichiello M; Saulino C; Auletta G; Giannini P; Donaudy F; Ciccodicola A; Gasparini P; Franzè A; Marciano E Audiol Neurootol; 2006; 11(3):157-64. PubMed ID: 16449806 [TBL] [Abstract][Full Text] [Related]
18. Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations. Cryns K; Pfister M; Pennings RJ; Bom SJ; Flothmann K; Caethoven G; Kremer H; Schatteman I; Köln KA; Tóth T; Kupka S; Blin N; Nürnberg P; Thiele H; van de Heyning PH; Reardon W; Stephens D; Cremers CW; Smith RJ; Van Camp G Hum Genet; 2002 May; 110(5):389-94. PubMed ID: 12073007 [TBL] [Abstract][Full Text] [Related]
19. A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment families. Alasti F; Sanati MH; Behrouzifard AH; Sadeghi A; de Brouwer AP; Kremer H; Smith RJ; Van Camp G Int J Pediatr Otorhinolaryngol; 2008 Feb; 72(2):249-55. PubMed ID: 18022253 [TBL] [Abstract][Full Text] [Related]
20. Clinical and genetic features of nonsyndromic autosomal dominant sensorineural hearing loss: KCNQ4 is a gene responsible in Japanese. Akita J; Abe S; Shinkawa H; Kimberling WJ; Usami S J Hum Genet; 2001; 46(7):355-61. PubMed ID: 11450843 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]